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Sensitive and Rapid Phenotyping of Microbes With Soluble Methane Monooxygenase Using a Droplet-Based Assay

Methanotrophs with soluble methane monooxygenase (sMMO) show high potential for various ecological and biotechnological applications. Here, we developed a high throughput method to identify sMMO-producing microbes by integrating droplet microfluidics and a genetic circuit-based biosensor system. sMM...

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Autores principales: Lee, Hyewon, Baek, Ji In, Kim, Su Jin, Kwon, Kil Koang, Rha, Eugene, Yeom, Soo-Jin, Kim, Haseong, Lee, Dae-Hee, Kim, Dong-Myung, Lee, Seung-Goo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7193049/
https://www.ncbi.nlm.nih.gov/pubmed/32391352
http://dx.doi.org/10.3389/fbioe.2020.00358
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author Lee, Hyewon
Baek, Ji In
Kim, Su Jin
Kwon, Kil Koang
Rha, Eugene
Yeom, Soo-Jin
Kim, Haseong
Lee, Dae-Hee
Kim, Dong-Myung
Lee, Seung-Goo
author_facet Lee, Hyewon
Baek, Ji In
Kim, Su Jin
Kwon, Kil Koang
Rha, Eugene
Yeom, Soo-Jin
Kim, Haseong
Lee, Dae-Hee
Kim, Dong-Myung
Lee, Seung-Goo
author_sort Lee, Hyewon
collection PubMed
description Methanotrophs with soluble methane monooxygenase (sMMO) show high potential for various ecological and biotechnological applications. Here, we developed a high throughput method to identify sMMO-producing microbes by integrating droplet microfluidics and a genetic circuit-based biosensor system. sMMO-producers and sensor cells were encapsulated in monodispersed droplets with benzene as the substrate and incubated for 5 h. The sensor cells were analyzed as the reporter for phenol-sensitive transcription activation of fluorescence. Various combinations of methanotrophs and biosensor cells were investigated to optimize the performance of our droplet-integrated transcriptional factor biosensor system. As a result, the conditions to ensure sMMO activity to convert the starting material, benzene, into phenol, were determined. The biosensor signals were sensitive and quantitative under optimal conditions, showing that phenol is metabolically stable within both cell species and accumulates in picoliter-sized droplets, and the biosensor cells are healthy enough to respond quantitatively to the phenol produced. These results show that our system would be useful for rapid evaluation of phenotypes of methanotrophs showing sMMO activity, while minimizing the necessity of time-consuming cultivation and enzyme preparation, which are required for conventional analysis of sMMO activity.
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spelling pubmed-71930492020-05-08 Sensitive and Rapid Phenotyping of Microbes With Soluble Methane Monooxygenase Using a Droplet-Based Assay Lee, Hyewon Baek, Ji In Kim, Su Jin Kwon, Kil Koang Rha, Eugene Yeom, Soo-Jin Kim, Haseong Lee, Dae-Hee Kim, Dong-Myung Lee, Seung-Goo Front Bioeng Biotechnol Bioengineering and Biotechnology Methanotrophs with soluble methane monooxygenase (sMMO) show high potential for various ecological and biotechnological applications. Here, we developed a high throughput method to identify sMMO-producing microbes by integrating droplet microfluidics and a genetic circuit-based biosensor system. sMMO-producers and sensor cells were encapsulated in monodispersed droplets with benzene as the substrate and incubated for 5 h. The sensor cells were analyzed as the reporter for phenol-sensitive transcription activation of fluorescence. Various combinations of methanotrophs and biosensor cells were investigated to optimize the performance of our droplet-integrated transcriptional factor biosensor system. As a result, the conditions to ensure sMMO activity to convert the starting material, benzene, into phenol, were determined. The biosensor signals were sensitive and quantitative under optimal conditions, showing that phenol is metabolically stable within both cell species and accumulates in picoliter-sized droplets, and the biosensor cells are healthy enough to respond quantitatively to the phenol produced. These results show that our system would be useful for rapid evaluation of phenotypes of methanotrophs showing sMMO activity, while minimizing the necessity of time-consuming cultivation and enzyme preparation, which are required for conventional analysis of sMMO activity. Frontiers Media S.A. 2020-04-24 /pmc/articles/PMC7193049/ /pubmed/32391352 http://dx.doi.org/10.3389/fbioe.2020.00358 Text en Copyright © 2020 Lee, Baek, Kim, Kwon, Rha, Yeom, Kim, Lee, Kim and Lee. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Lee, Hyewon
Baek, Ji In
Kim, Su Jin
Kwon, Kil Koang
Rha, Eugene
Yeom, Soo-Jin
Kim, Haseong
Lee, Dae-Hee
Kim, Dong-Myung
Lee, Seung-Goo
Sensitive and Rapid Phenotyping of Microbes With Soluble Methane Monooxygenase Using a Droplet-Based Assay
title Sensitive and Rapid Phenotyping of Microbes With Soluble Methane Monooxygenase Using a Droplet-Based Assay
title_full Sensitive and Rapid Phenotyping of Microbes With Soluble Methane Monooxygenase Using a Droplet-Based Assay
title_fullStr Sensitive and Rapid Phenotyping of Microbes With Soluble Methane Monooxygenase Using a Droplet-Based Assay
title_full_unstemmed Sensitive and Rapid Phenotyping of Microbes With Soluble Methane Monooxygenase Using a Droplet-Based Assay
title_short Sensitive and Rapid Phenotyping of Microbes With Soluble Methane Monooxygenase Using a Droplet-Based Assay
title_sort sensitive and rapid phenotyping of microbes with soluble methane monooxygenase using a droplet-based assay
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7193049/
https://www.ncbi.nlm.nih.gov/pubmed/32391352
http://dx.doi.org/10.3389/fbioe.2020.00358
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